http://identifiers.org/hco/7/GRCh38#143851486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42645047-C-A

143851553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42645104-G-T

143851680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42645236-T-C

143851819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42645365-A-G

143851866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42645406-T-C

http://identifiers.org/hco/7/GRCh38#143851936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42645480-C-A

143851962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42645506-T-C

143852550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646059-T-G

143852639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646142-A-G

143852800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646263-T-C

143852808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646271-G-T

143852889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646333-C-T

143852899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646343-G-C

143852910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646354-C-G

143852979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646422-A-T

143853000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646443-T-G

143853014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646457-T-C

143853533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646695-T-G

143853741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42646869-G-T

143853991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42647107-G-T

143854260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42647371-G-A

143854584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42647859-G-T

143854656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42647931-T-C

143856823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650034-T-C

http://identifiers.org/hco/7/GRCh38#143856967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42650178-C-A

143856967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650178-C-G

143856967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650178-C-T

143856996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650208-G-A

143856996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650208-G-T

143857045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650258-C-T

143857270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42650483-A-G

143857424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650639-G-C

143857424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650639-G-T

http://identifiers.org/hco/7/GRCh38#143857466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42650681-A-C

143857466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650681-A-G

http://identifiers.org/hco/7/GRCh38#143857471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42650686-C-A

143857471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650686-C-T

143857472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650687-G-A

143857472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650687-G-T

http://identifiers.org/hco/7/GRCh38#143857541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42650743-C-A

http://identifiers.org/hco/7/GRCh38#143857594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42650788-C-A

143857618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650806-T-C

143857634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650822-C-T

143857809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42650980-A-G

143858164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651340-G-A

143858207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651370-G-T

143858211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651374-C-G

143858277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651440-G-C

143858403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651562-C-T

143858414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651576-G-A

143858438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651589-T-C

143858532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651684-G-C

143858532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651684-G-T

143858599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651752-G-A

143858636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651799-C-T

143858743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651901-G-A

143858801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42651953-C-T

143858896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42652048-G-C

143859076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42652228-C-T

143859121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42652273-C-T

http://identifiers.org/hco/7/GRCh38#143859145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42652297-C-A

143859145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42652297-C-G

143859145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42652297-C-T

http://identifiers.org/hco/7/GRCh38#143859176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42652327-A-C

143860103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42653629-G-A

143860103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42653629-G-T

http://identifiers.org/hco/7/GRCh38#143860104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42653630-C-A

143860104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42653630-C-T

143860141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42653668-A-G

143860165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42653687-G-A

143860165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42653687-G-T

http://identifiers.org/hco/7/GRCh38#143860201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42653718-C-A

143860335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42653852-A-G

143860385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42653902-G-T

143860538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42654067-T-C

143861276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42654445-G-A

143861276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42654445-G-T

143862207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42654809-G-T

http://identifiers.org/hco/7/GRCh38#143862668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42655237-C-A

143862733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42655302-A-T

http://identifiers.org/hco/7/GRCh38#143863940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42656488-C-A

143863940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42656488-C-G

143864525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42657011-G-C

143874493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42661793-G-C

143874877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662212-A-G

143874987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662322-T-A

143874987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662322-T-C

143875034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662369-T-C

143875284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662589-T-C

http://identifiers.org/hco/7/GRCh38#143875399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42662690-A-C

143875399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662690-A-G

143875422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662714-T-C

143875429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662721-A-G

143875506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42662811-C-T

143875741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663036-C-T

http://identifiers.org/hco/7/GRCh38#143875775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42663072-A-C

http://identifiers.org/hco/7/GRCh38#143875876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42663152-C-A

143875893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663166-G-A

143875893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663166-G-T

143875905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663178-G-A

143875905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663178-G-T

http://identifiers.org/hco/7/GRCh38#143876093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42663363-C-A

143876093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42663363-C-G

143876093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42663363-C-T

143876103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42663373-G-A

143876103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42663373-G-T

143876141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42663411-A-G

143876438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42663708-G-A

143876438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42663708-G-T

143876662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663933-G-A

143876662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663933-G-T

http://identifiers.org/hco/7/GRCh38#143876705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42663975-C-A

143876705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42663975-C-T

143876792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664018-C-T

143876878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664091-A-G

143877154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664347-C-T

143877201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664404-C-G

143877201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664404-C-T

143877215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664418-G-A

143877272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664669-C-T

143877316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664711-T-C

143877359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664755-A-T

143877501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42664887-C-T

143878211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665095-G-C

143878458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665344-G-T

143878460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665346-C-T

143878529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665431-A-G

http://identifiers.org/hco/7/GRCh38#143878601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42665713-C-A

143878601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665713-C-T

143878642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665755-C-T

143878678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665795-T-C

143878738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665850-A-T

143878768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42665881-T-G

143878897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666009-T-C

143879181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666286-T-C

143879635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666552-A-G

143879827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666736-G-C

143879896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666800-C-T

143880028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666915-G-A

143880087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42666967-A-G

143880138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42667006-T-C

143880150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42667014-G-A

143880289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42667149-G-T

143880321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42667182-C-T

143880475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42667968-T-G

143880987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668084-T-C

143881110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668200-C-G

143881284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668354-A-T

143881423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668487-T-C

143881523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668614-T-G

143881680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42668767-C-G

http://identifiers.org/hco/7/GRCh38#143881940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669045-C-A

143881940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669045-C-T

143881945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669050-T-C

143881957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669065-G-A

http://identifiers.org/hco/7/GRCh38#143881971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669083-C-A

http://identifiers.org/hco/7/GRCh38#143882026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669135-C-A

143882028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669137-G-A

143882028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669137-G-T

143882030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669139-G-T

143882044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669153-A-G

143882413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669531-G-A

143882413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669531-G-C

http://identifiers.org/hco/7/GRCh38#143882454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669572-C-A

143882501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669633-G-A

143882501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669633-G-C

143882535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669670-C-T

143882568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669707-T-A

143882568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669707-T-C

143882568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669707-T-G

143882569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669708-C-T

http://identifiers.org/hco/7/GRCh38#143882603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669731-C-A

143882603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669731-C-T

http://identifiers.org/hco/7/GRCh38#143882619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669747-C-A

143882619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669747-C-T

http://identifiers.org/hco/7/GRCh38#143882622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669750-C-A

143882622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669750-C-G

143882625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669761-G-A

143882625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669761-G-C

143882625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669761-G-T

143882691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42669827-T-G

143882765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669890-G-A

143882793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669916-G-A

http://identifiers.org/hco/7/GRCh38#143882794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669917-A-C

143882794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669917-A-G

http://identifiers.org/hco/7/GRCh38#143882803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42669926-C-A

143882854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669984-G-A

143882854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669984-G-T

143882862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669992-G-A

143882862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42669992-G-T

143882870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42670000-T-C

143882870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42670000-T-G

143882871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42670001-G-A

143882927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42670052-A-G

143882961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670085-G-A

143882961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670085-G-T

143883017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670141-T-C

143883055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670184-G-A

143883055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670184-G-T

143883088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670209-T-C

143883118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670251-T-C

http://identifiers.org/hco/7/GRCh38#143883964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42670712-C-A

143884035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42670773-C-T

143884328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671119-T-C

143885036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671771-G-T

http://identifiers.org/hco/7/GRCh38#143885083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42671797-A-C

143885083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671797-A-G

143885105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671815-T-C

http://identifiers.org/hco/7/GRCh38#143885119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42671829-C-A

143885119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671829-C-G

143885121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671831-T-A

143885123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671833-A-G

http://identifiers.org/hco/7/GRCh38#143885129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42671839-C-A

143885129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42671839-C-T

143885152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671860-T-A

143885152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671860-T-C

143885192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671901-G-A

143885192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42671901-G-T

http://identifiers.org/hco/7/GRCh38#143885219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42671926-C-A

143885219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671926-C-T

143885221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671928-G-A

143885221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671928-G-C

143885221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671928-G-T

143885234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671942-C-G

143885234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42671942-C-T

143885259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42671979-T-G

143885311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42672026-T-C

143885311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42672026-T-G

143885342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42672035-G-T

143885344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42672037-G-A

143885426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, undefined
orthologous variants: 42672097-G-C

143885426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, undefined
orthologous variants: 42672097-G-T

http://identifiers.org/hco/7/GRCh38#143885626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42672334-A-C

143885638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42672346-G-A

http://identifiers.org/hco/7/GRCh38#143886032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42673000-C-A

http://identifiers.org/hco/7/GRCh38#143886091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42673058-A-C

143886092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673059-C-T

143886125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673095-T-C

143886151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673121-G-A

143886241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673196-C-T

143886244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673199-C-T

143886369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673258-G-T

143886374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673263-A-G

http://identifiers.org/hco/7/GRCh38#143886442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42673330-C-A

143886471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673359-C-G

143886471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42673359-C-T

143886526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42673417-T-C

143886527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42673418-A-G

143887310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42674447-G-A

143887310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42674447-G-T

143887673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42674649-C-T

http://identifiers.org/hco/7/GRCh38#143888135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42675730-C-A

143888334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42675918-T-C

143888357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42675940-G-A

143888501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676033-T-C

143888693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676222-A-G

143888693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676222-A-T

143888966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42676509-T-C

143899903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42684846-T-C

143900547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685471-G-A

143900580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685500-C-G

143900771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685671-T-C

143900959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685837-T-C

143901144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685993-G-A

143901144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42685993-G-T

143901161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686012-T-A

143901305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686160-C-G

143901582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686447-T-C

143901582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686447-T-G

143901723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686594-T-C

143901911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686780-A-G

143901952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686816-G-A

143901952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42686816-G-C

143901984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42686849-G-A

http://identifiers.org/hco/7/GRCh38#143902010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42686876-C-A

143902010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42686876-C-G

143902010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42686876-C-T

http://identifiers.org/hco/7/GRCh38#143902017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42686883-C-A

143902018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42686884-C-T

http://identifiers.org/hco/7/GRCh38#143902038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42686902-C-A

143902082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5 prime UTR variant
orthologous variants: 42686940-A-G

143902192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42687034-G-A

143902192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42687034-G-C

143902192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22201
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42687034-G-T